Canonical Allele Identifier: PA2826955738
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 515481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro106Arg
CA10558583
NM_001316337.2:c.317C>G